17 results on '"Martin, Clémence"'
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2. Gathering real-world compassionate data to expand eligibility for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with N1303K or other rareCFTRvariants: a viewpoint
3. Theratyping cystic fibrosis patients to guide elexacaftor/tezacaftor/ivacaftor out-of-label prescription
4. The French Compassionate Program of elexacaftor-tezacaftor-ivacaftor in people with cystic fibrosis with advanced lung disease and no F508delCFTRvariant
5. Normalisation of circulating neutrophil counts after 12 months of elexacaftor-tezacaftor-ivacaftor in patients with advanced cystic fibrosis
6. Reclassifying inconclusive diagnosis for cystic fibrosis with new generation sweat test
7. Using chest CT scan and unsupervised machine learning for predicting and evaluating response to lumacaftor-ivacaftor in people with cystic fibrosis
8. Improved survival albeit with persistent disparities in prognosis for people with cystic fibrosis in European countries
9. Involvement of CFTR in the pathogenesis of pulmonary arterial hypertension
10. Effective control ofStaphylococcus aureuslung infection despite tertiary lymphoid structure disorganisation
11. Carriers of a single CFTR mutation are asymptomatic: an evolving dogma?
12. Cured bronchi! Extending the use of nebulised hypertonic saline outside of cystic fibrosis?
13. Bacteria-driven peribronchial lymphoid neogenesis in bronchiectasis and cystic fibrosis
14. CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium
15. Gathering real-world compassionate data to expand eligibility for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with N1303K or other rare CFTR variants: a viewpoint.
16. Normalisation of circulating neutrophil counts after 12 months of elexacaftor-tezacaftor-ivacaftor in patients with advanced cystic fibrosis.
17. Effective control of Staphylococcus aureus lung infection despite tertiary lymphoid structure disorganisation.
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